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Author Details
Full Name
Aaron K Wong
Affiliation
Flatiron Institute, Simons Foundation
ORCID
Career Start Year
2004
Papers
38
H Index
24
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37703883
Atlas of primary cell-type-specific sequence models of gene expression and variant effects.
Cell Rep Methods
2023
35817977
A sequence-based global map of regulatory activity for deciphering human genetics.
Nat Genet
2022
35477557
Molecular Characterization of Membranous Nephropathy.
J Am Soc Nephrol
2022
33462483
Genome-wide landscape of RNA-binding protein target site dysregulation reveals a major impact on psychiatric disorder risk.
Nat Genet
2021
33888512
Modeling transcriptional regulation of model species with deep learning.
Genome Res
2021
33689683
Tissue-specific enhancer functional networks for associating distal regulatory regions to disease.
Cell Syst
2021
34428401
Spatial transcriptional mapping of the human nephrogenic program.
Dev Cell
2021
34341555
Decoding disease: from genomes to networks to phenotypes.
Nat Rev Genet
2021
32511461
SARS-CoV-2 receptor networks in diabetic and COVID-19 associated kidney disease.
medRxiv
2020
33038424
SARS-CoV-2 receptor networks in diabetic and COVID-19-associated kidney disease.
Kidney Int
2020
31133750
Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk.
Nat Genet
2019
30478325
Interpretation of an individual functional genomics experiment guided by massive public data.
Nat Methods
2018
29800226
GIANT 2.0: genome-scale integrated analysis of gene networks in tissues.
Nucleic Acids Res
2018
30013180
Deep learning sequence-based ab initio prediction of variant effects on expression and disease risk.
Nat Genet
2018
30003887
Enabling Precision Medicine through Integrative Network Models.
J Mol Biol
2018
30346941
An integrative tissue-network approach to identify and test human disease genes.
Nat Biotechnol
2018
26788126
Network-based analysis of genetic variants associated with hippocampal volume in Alzheimer's disease: a study of ADNI cohorts.
BioData Min
2016
27479844
Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder.
Nat Neurosci
2016
27098035
GIANT API: an application programming interface for functional genomics.
Nucleic Acids Res
2016
25581801
Targeted exploration and analysis of large cross-platform human transcriptomic compendia.
Nat Methods
2015
26362267
Interactive Big Data Resource to Elucidate Human Immune Pathways and Diseases.
Immunity
2015
25915600
Understanding multicellular function and disease with human tissue-specific networks.
Nat Genet
2015
25969450
IMP 2.0: a multi-species functional genomics portal for integration, visualization and prediction of protein functions and networks.
Nucleic Acids Res
2015
25940632
FNTM: a server for predicting functional networks of tissues in mouse.
Nucleic Acids Res
2015
25786808
Low-variance RNAs identify Parkinson's disease molecular signature in blood.
Mov Disord
2015
25431329
Tissue-aware data integration approach for the inference of pathway interactions in metazoan organisms.
Bioinformatics
2015
23134432
A de novo mutation in KIT causes white spotting in a subpopulation of German Shepherd dogs.
Anim Genet
2013
23516347
Functional knowledge transfer for high-accuracy prediction of under-studied biological processes.
PLoS Comput Biol
2013
22684505
IMP: a multi-species functional genomics portal for integration, visualization and prediction of protein functions and networks.
Nucleic Acids Res
2012
23028291
Tissue-specific functional networks for prioritizing phenotype and disease genes.
PLoS Comput Biol
2012
23134304
Marker panels for genealogy-based mapping, breed demographics, and inference-of-ancestry in the dog.
Anim Biotechnol
2012
20080661
Tracking footprints of artificial selection in the dog genome.
Proc Natl Acad Sci U S A
2010
20862248
An ADAMTSL2 founder mutation causes Musladin-Lueke Syndrome, a heritable disorder of beagle dogs, featuring stiff skin and joint contractures.
PLoS One
2010
20403140
Necrotizing meningoencephalitis of Pug dogs associates with dog leukocyte antigen class II and resembles acute variant forms of multiple sclerosis.
Tissue Antigens
2010
19966068
A comprehensive linkage map of the dog genome.
Genetics
2010
19392818
DOGSET: pre-designed primer sets for fine-scale mapping and DNA sequence interrogation in the dog.
Anim Genet
2009
19713490
Coat variation in the domestic dog is governed by variants in three genes.
Science
2009
15289602
Breed distribution and history of canine mdr1-1Delta, a pharmacogenetic mutation that marks the emergence of breeds from the collie lineage.
Proc Natl Acad Sci U S A
2004
1 - 38 of 38
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